Solute carrier family 38 member 9

SLC38A9
Identifiers
Aliases	SLC38A9, URLC11, solute carrier family 38 member 9
External IDs	OMIM: 616203; MGI: 1918839; HomoloGene: 18139; GeneCards: SLC38A9; OMA:SLC38A9 - orthologs
Gene location (Human)
Chr.	Chromosome 5 (human)
End	55,773,194 bp
Gene location (Mouse)
Chr.	Chromosome 13 (mouse)
End	112,875,283 bp
RNA expression pattern
	Top expressed in
	secondary oocyte; ; placenta; ; pancreatic epithelial cell; ; buccal mucosa cell; ; Achilles tendon; ; tibia; ; body of pancreas; ; germinal epithelium; ; gonad; ; bone marrow cells;
	Top expressed in
	lumbar spinal ganglion; ; spermatid; ; spermatocyte; ; bone marrow; ; otolith organ; ; utricle; ; hand; ; secondary oocyte; ; seminal vesicula; ; pineal gland;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding; amino acid transmembrane transporter activity; L-leucine transmembrane transporter activity; L-arginine transmembrane transporter activity; metal ion binding;
Cellular component	integral component of membrane; endosome; Ragulator complex; late endosome; lysosome; membrane; late endosome membrane; nucleoplasm; intracellular membrane-bounded organelle; lysosomal membrane; integral component of lysosomal membrane;
Biological process	cellular response to amino acid stimulus; amino acid transmembrane transport; amino acid transport; positive regulation of TOR signaling; regulation of macroautophagy; branched-chain amino acid transport; neutral amino acid transport; cation transmembrane transport; L-alpha-amino acid transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	153129
	268706
	ENSG00000177058
	ENSMUSG00000047789
	Q8NBW4
	Q8BGD6
NM_001258286; NM_001258287; NM_001282429; NM_173514; NM_001349382;
	NM_001349383; NM_001349384; NM_001349385
	NM_175376; NM_178746
NP_001245215; NP_001245216; NP_001269358; NP_775785; NP_001336311;
	NP_001336312; NP_001336313; NP_001336314
	NP_848861
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 38 member 9 is a protein that in humans is encoded by the SLC38A9 gene.